Characterization and analysis of branched-chain N-acetylglucosaminyl oligosaccharides accumulating in Sandhoff disease tissue. Evidence that biantennary bisected oligosaccharide side chains of glycoproteins are abundant substrates for lysosomes.-Reference-Cited by-同舟云学术

Characterization and analysis of branched-chain N-acetylglucosaminyl oligosaccharides accumulating in Sandhoff disease tissue. Evidence that biantennary bisected oligosaccharide side chains of glycoproteins are abundant substrates for lysosomes.

Published:1985-05 Issue:10 Volume:260 Page:6194-6199
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Warner T G,deKremer R D,Sjoberg E R,Mock A K

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference29 articles.

1. GENETIC DEFECTS IN GLYCOPROTEIN METABOLISM

2. Urinary oligosaccharides of GM1-gangliosidosis. Structures of oligosaccharides excreted in the urine of type 1 but not in the urine of type 2 patients.

3. Urinary oligosaccharides of GM1-gangliosidosis. Different excretion patterns of oligosaccharides in the urine of type 1 and type 2 subgroups.

4. Urinary glycopeptides of fucosidosis.

5. Urinary oligosaccharides of mannosidosis.

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Natural history study of glycan accumulation in large animal models of GM2 gangliosidoses;PLOS ONE;2020-12-01

2. Analysis of urinary oligosaccharides in lysosomal storage disorders by capillary high-performance anion-exchange chromatography–mass spectrometry;Analytical and Bioanalytical Chemistry;2012-04-20

3. Lysosomal storage of oligosaccharide and glycosphingolipid in imino sugar treated cells;Glycoconjugate Journal;2010-02-26

4. A mass spectrometric strategy for profiling glycoproteinoses, Pompe disease, and sialic acid storage diseases;PROTEOMICS – CLINICAL APPLICATIONS;2008-04

5. MRS reveals additional hexoseN-acetyl resonances in the brain of a mouse model for Sandhoff disease;NMR in Biomedicine;2005-12